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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443794Generated: October 30, 2026

Water → 7-chloro-3-dipropylacetoxy-5-(2'-fluorophenyl)-1,3-dihydro-2H-1,4-benzodiazepine-2-one

https://huagongshe.com/reaction/443794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Propylpentanoyl 2-propylpentanoateHCID 10923624—
ReactantAcetone cyclohexaneHCID 21916603—
ReactantHCID 178516821HCID 178516821—
SolventChloroformHCID 6212—
Product7-chloro-3-dipropylacetoxy-5-(2'-fluorophenyl)-1,3-dihydro-2H-1,4-benzodiazepine-2-oneHCID 23465565—

Reaction Steps

A suspension of 10 g of 7-chloro-5-(2'-fluoro-phenyl)-1,3-dihydro-2H-1,4-benzodiazepine-2-one-4-oxide in 20 ml of absolute chloroform is mixed with 14.3 g of dipropyl acetic acid anhydride and is heated under reflux and with the exclusion of atmospheric moisture for such a length of time until a sample on the thin layer-chromatogram (silica gel 60 F 254 of the firm Merck, flow agent: cyclohexane/acetone=1:1) shows a complete conversion. Then, the cooled mixture is shaken out several times with water, the organic phase is dried with Na2SO4 and the filtrate is evaporated in the vacuum. Upon standing over night, the residue crystallizes, is washed with petroleum ether and recrystallized from aceontrile. One will obtain a colorless powder of 7-chloro-3-dipropylacetoxy-5-(2'-fluorophenyl)-1,3-dihydro-2H-1,4-benzodiazepine-2-one, which melts at 147°-149°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04261987
Source datasetuspto-grants-1981_04
ORD IDord-7a5b95c8da074024975d6528edeb2885
Source noteuspto-grants-1981_04